Canonical Allele Identifier: CA868715966

Gene: FBP1

Linked Data

• dbSNP Id: rs1301116361
• MyVariant Identifiers: chr9:g.97401684C>T (hg19) ; chr9:g.94639402C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.94639402C>T , CM000671.2:g.94639402C>T	GRCh38
NC_000009.11:g.97401684C>T , CM000671.1:g.97401684C>T	GRCh37
NC_000009.10:g.96441505C>T	NCBI36
NG_008174.1:g.5848G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375326.9:c.-92G>A MANE Select	ENSP00000364475.5:n.-92G>A
ENST00000375326.8:c.-92G>A	ENSP00000364475.4:n.-92G>A
ENST00000414122.1:c.-83+642G>A	ENSP00000411619.1:n.-83+642G>A
ENST00000415431.5:c.-24-68G>A	ENSP00000408025.1:n.-24-68G>A
NM_000507.3:c.-92G>A	NP_000498.2:n.-92G>A
NM_001127628.1:c.-24-68G>A	NP_001121100.1:n.-24-68G>A
XM_006717005.2:c.-77+642G>A	XP_006717068.1:n.-77+642G>A
XM_006717005.4:c.-77+642G>A	XP_006717068.1:n.-77+642G>A
NM_000507.4:c.-92G>A MANE Select	NP_000498.2:n.-92G>A
NM_001127628.2:c.-24-68G>A	NP_001121100.1:n.-24-68G>A